People with ALS are at an increased risk for respiratory problems associated with viral infections.
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Donate- Please be assured that the work of the ALS Association will continue.
- Our first priority is the safety and well-being of people with ALS, their families and caregivers, and our staff.
- Chapter staff will be working remotely and still available to our constituents daily.
- We anticipate that some activities may need to be cancelled, modified or rescheduled; we will communicate with you directly regarding changes to upcoming plans, so please watch your email.
- You can find the latest updates about our activities on our Facebook and Twitter pages.
- For the most recent information about the coronavirus (COVID-19), The ALS Association recommends that you reference the websites for the Centers for Disease Control (CDC), the World Health Organization (WHO), and state and local health authorities.
For specific information about symptoms you may be experiencing or questions about personal exposure as someone living with ALS or as a caregiver, please contact your physician directly.
Thank you for your patience as we manage this rapidly shifting situation.
National ALS Registry
The National ALS Registry is a congressionally mandated registry for persons in the U.S. with ALS. It is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes.
Learn More
ALS Research Update Featuring Suma Babu, MBBS, MPH
Research Update provides a platform for patients, families and the community to learn about and discuss current trends in ALS treatment and research. This is a free event with complimentary dinner and the opportunity to meet vendors and supporters of the ALS Association Indaina Chapter who are working to improve the lives of all those affected by ALS. More Information Click Here
Walk to Defeat ALS
Walk to Defeat ALS® draws people of all ages and athletic abilities together to honor the courageous souls who are affected by ALS, to remember those who have passed, and to show support for the cause. When you Walk to Defeat ALS©, you help expand the programs and services that benefit people living with the disease across the nation and in your community.
Find A Walk Near You
Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.
For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.
For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.
For Caregivers- How The ALS Association’s is Pursuing 2020 Public Policy Priorities During the COVID-19 Pandemic
March 26, 2020 - The ALS Association Furthers Commitment to Develop Technologies to Help People with ALS Live Better
March 25, 2020 - The Jane Calmes ALS Scholarship Fund Kicks Off Year Two
March 24, 2020 - Questions and Answers about COVID-19 and Its Impact on People with ALS
March 23, 2020
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Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.